Medical writing
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Medical writing

RDG services of medical and regulatory writing are including:

  • Product development plan
  • CTD
  • Pharmaceutical section of common technical documents (CTD)
  • Normative document
  • Regulatory applications
  • Clinical development plan
  • Protocols
  • CRFs
  • Investigator brochures
  • Informed consent forms
  • Clinical study reports
  • Clinical sections of common technical documents (CTD)
  • Abstracts, journal articles
  • Periodic safety update reports (PSURs) and other pharmacovigilance documents
  • Preclinical study report
  • Medical and/or scientific literature review